Canonical Allele Identifier: CA392973360

Gene: CLN6

Linked Data

• gnomAD v4: 15-68211703-A-G
• MyVariant Identifiers: chr15:g.68504041A>G (hg19) ; chr15:g.68211703A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68211703A>G , CM000677.2:g.68211703A>G	GRCh38
NC_000015.9:g.68504041A>G , CM000677.1:g.68504041A>G	GRCh37
NC_000015.8:g.66291095A>G	NCBI36
NG_008764.2:g.50509T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000249806.11:c.458T>C MANE Select	ENSP00000249806.5:p.Ile153Thr
ENST00000562767.2:c.84-14075T>C	ENSP00000456336.1:n.84-14075T>C
ENST00000563917.2:n.300T>C
ENST00000565471.6:c.84-1944T>C	ENSP00000457384.1:n.84-1944T>C
ENST00000635747.1:c.*361T>C	ENSP00000490627.1:n.*361T>C
ENST00000636212.1:c.*9T>C	ENSP00000489851.1:n.*9T>C
ENST00000636314.1:c.183-385T>C	ENSP00000490295.1:n.183-385T>C
ENST00000636674.1:n.1441T>C
ENST00000636964.1:n.1630T>C
ENST00000637054.1:c.198+6833T>C	ENSP00000490807.1:n.198+6833T>C
ENST00000637223.1:c.*201-385T>C	ENSP00000490010.1:n.*201-385T>C
ENST00000637329.1:c.427T>C
ENST00000637450.1:c.*112T>C	ENSP00000490204.1:n.*112T>C
ENST00000637494.1:c.199-385T>C	ENSP00000490057.1:n.199-385T>C
ENST00000637667.1:c.359T>C	ENSP00000489843.1:p.Ile120Thr
ENST00000637823.1:c.224-60T>C
ENST00000637888.1:c.198+6833T>C	ENSP00000490546.1:n.198+6833T>C
ENST00000638076.1:c.458T>C	ENSP00000490373.1:p.Ile153Thr
ENST00000638144.1:n.130-385T>C
ENST00000646164.1:c.38+6833T>C
ENST00000249806.9:c.458T>C	ENSP00000249806.5:p.Ile153Thr
ENST00000538696.5:c.554T>C	ENSP00000445770.1:p.Ile185Thr
ENST00000562767.1:c.84-14075T>C	ENSP00000456336.1:n.84-14075T>C
ENST00000563917.1:n.239T>C
ENST00000564752.1:c.458T>C	ENSP00000457822.1:p.Ile153Thr
ENST00000565471.5:c.84-1944T>C	ENSP00000457384.1:n.84-1944T>C
ENST00000566347.5:c.298-385T>C	ENSP00000457783.1:n.298-385T>C
ENST00000567060.5:c.298-1983T>C	ENSP00000454818.1:n.298-1983T>C
NM_017882.2:c.458T>C	NP_060352.1:p.Ile153Thr
XR_931861.1:n.561T>C
NM_017882.3:c.458T>C MANE Select	NP_060352.1:p.Ile153Thr